Abstract

Abstract Adjuvants function as "immunologists' dirty tricks" for enhancement of immune response. However, no two adjuvants work in a similar fashion. Adjuvant efficacy depends on how they influence microenvironment, antigen presentation and retention of immunogens. We are developing water-in-oil emulsion-type adjuvants from phytol (J Immune Based Ther Vaccines 2006, 5:4; ibid 2007; 5: 3). Phytol is a diterpene present in chlorophylls, alpha-tocopherols etc. Phytol derivatives we developed are hydrogenated/nitrated and glycosylated products (US patent pending). Our previous study showed that one phytol derivative PHIS-01(hydrogenated) is an excellent non-toxic adjuvant. In this study, we investigated the safety and efficacy of two other phytol compounds, PHIS-02 and PHIS-03 relative to PHIS-01 and other adjuvants. Using phthalate- keyhole limpet hemocyanin (KLH) conjugate as the immunogen emulsified with these adjuvants, we assessed titer, specificity, and isotypic profiles of anti-phthalate antibodies induced. In addition, we studied their effects on cellular immunity such as T cell proliferation and cytokine production. Preliminary results show that (1) phytol adjuvants significantly augment antibody response of isotypes IgG1 and IgG2a, (2) promote effective T cell proliferation, and (3) exhibit low toxicity with no adverse autoimmune anti-DNA response. We also observed that these adjuvants exert apoptotic/necrotic effects on mouse lymphoma cells 2C3 and A20 in a concentration-dependent manner.

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